Iranian psoriasis registry: Research protocol and preliminary results of a pilot study

Male Adult Humans Psoriasis Female Pilot Projects Registries Iran Child 3. Good health
DOI: 10.1111/jocd.16046 Publication Date: 2023-11-06T10:35:22Z
ABSTRACT
Abstract Background Psoriasis as a common cutaneous inflammatory disease affect many aspects of patients' life. Disease registries render it possible to collect valuable data regarding prevalence and burden well long‐term observations concerning therapeutic regimens. Methods This registry was designed for the ongoing systematic collection on patients with psoriasis at two referral dermatology centers in Iran. The pilot phase used identify obstacles application execution registration. Results A total 281 were registered mean age 42.02 years. duration 12.06 ± 10.90 years variety clinical presentations. There no significant difference between males females onset ( p = 0.53). Notably, 167 had children. Among them, 13 children psoriasis. gender affected parent did not possibility transmission child, seen sexes (P 0.569). Regarding treatment, 99.4% (n 280) topical agents, 52.3% 147) biologics, 60.9% 171) nonbiologic medications. Conclusion Clinical trials report efficacy safety limited study populations restricted time window, results may differ from general population. highlights importance registry‐based studies collecting analyzing longitudinal information. In terms complications such malignancies, cardiovascular events, serious adverse will help clinicians better recognize manage each disease.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (20)
CITATIONS (0)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....